Coating formulations for scoring or cutting balloon catheters

ABSTRACT

The present invention is related to scoring or cutting balloon catheters carrying at least on a portion of their surface at least one oxidation-insensitive drug or oxidation-insensitive polymer-free drug preparation and at least one lipophilic antioxidant at a ratio of 3-100% by weight of the at least one lipophilic antioxidant in relation to 100% by weight of the drug, wherein the at least one oxidation-insensitive drug is selected of taxanes, thalidomide, statins, corticoids and lipophilic derivatives of corticoids, and the at least one lipophilic antioxidant is selected of nordihydroguaiaretic acid, resveratrol and propyl gallate.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of PCT Application No.PCT/EP2010/066754, filed Nov. 3, 2010, which claims the benefit of EPApplication No. 10160347.0, filed Apr. 19, 2010, the full disclosures ofwhich are incorporated herein by reference in their entirety.

BACKGROUND

1. Field of the Invention

The invention relates to the transfer of a drug loosely adhering to thesurface of a scoring or cutting balloon catheter to a site inside thebody, usually in a diseased blood vessel. The preferred application islocal drug therapy during percutaneous transluminal angioplasty (PTA) orpercutaneous transluminal coronary angioplasty (PTCA). The interventionsare performed to restore blood flow in stenotic or occluded bloodvessels, usually into arteries. A catheter is introduced in a majorartery. At the distal end the catheter carries a cylindrical balloon infolded state with very small diameter and additional tools or structureswhich scratch or cut the luminal surface of the treated blood vessel ortissue. In the folded state the balloon can enter or pass the stenoticor occluded segment of e.g. a blood vessel. Once positioned in thenarrowed segment, the balloon is inflated to enlarge the lumen of theblood vessel to its original diameter. Simultaneously, a drug may betransferred to the vessel wall to prevent early and late re-narrowingdue to hyperproliferation of the injured vessel wall.

Medical devices may contain drugs either to improve the tolerance,efficacy or in vivo life-time of the device or the device serves ascarrier for the drug. In any case the dose density (e.g. mg drug/mgdevice or mg drug/mm² device surface), chemical stability, adherence,release rate, and total amount released are important and frequentlycritical features of the drug formulation. These properties are the morecritical the more the requirements during production and application ofthe device vary or may even be contradictory. Drug-coated angioplastycatheters are typical examples: the drug coating must adhere firmly totolerate mechanical stress during production including folding ofballoons, crimping of stents, packaging, transportation to customers,and during final application, which involves the passage through anarrow hemostatic valve, an introductory sheath or guiding catheter anda variable distance through possibly tortuous and narrow blood vessels.When the balloon is inflated the drug should be released within a minuteor less as rapidly and as completely as possible. The problem wasdemonstrated by Cremers et al. (Cremers B, Biedermann M, Mahnkopf D,Bdhm M, Scheller B. Comparison of two different paclitaxel-coatedballoon catheters in the porcine coronary restenosis model. Clin ResCardiol 2009; 98:325-330) who retrieved as much as 50% of the dose fromballoons after expansion for one minute in coronary arteries of pigs,whereas other catheters coated with the same drug and dose but in adifferent formulation released more than 95%. Almost perfect results(i.e., loss of only 10% of dose and residual drug on the balloon afterexpansion in an artery of about 10%) were achieved with a rigidprototype balloon (Scheller B, Speck U, Abramjuk C, Bernhardt U, Bohm M,Nickenig G. Paclitaxel balloon coating—a novel method for prevention andtherapy of restenosis. Circulation 2004; 110: 810-814). The applicationof the same coating composition to more flexible modern ballooncatheters resulted in problems, i.e., larger premature loss of the drug.The coating of scoring or cutting balloons with drugs in a reliable waywith a dose which is sufficient to be efficacious imposes additionalproblems because of the more com-plex structure of the device and themore complex production process.

2. Prior Art

Protection from premature drug release. Premature release of a drug froma balloon is a major problem which has been addressed by a variety ofmethods. Some of them are mechanical, e.g. the use of protection tubes,sleeves, envelops. Examples are U.S. Pat. Nos. 5,370,614, 6,306,166, and6,616,650 disclosing various protective sheaths which are retractedbefore the balloon is inflated, or U.S. Pat. No. 6,419,692 proposing acover which bursts during balloon expansion. A different approach istaken in U.S. Pat. No. 5,893,840 disclosing structured balloon membraneswith tiny cavities, WO 94/23787 with roughened balloon membranes toenhance the adherence of coating, or more recently U.S. Pat. No.7,108,684 proposing a pouch which protects the drug-containing layer onthe balloon and WO 2009/066330 disclosing methods placing the drugselectively under the folds of a folded balloon. Although efficaciousthese methods have the disadvantage of increasing the complexity andcost of production or make handling of the devices more difficult or addto the diameter of the devices (which must be kept as small as possibleto facilitate passage through stenotic lesions). In some embodiments theprotective membranes or perforated membranes interfere with the scoringcomponents of the balloons or prevent a homogeneous transfer of the drugto the tissue or even put the patient at risk. None of these methods hasbeen applied to scoring or cutting balloons and nothing is known aboutproblems which will arise from the increasing complexity and mechanicalproblems or from a disturbance of the protecting envelops by the scoringor cutting structures and vice-versa.

Other approaches use either physical or chemical methods to control therelease of drugs from a balloon surface, e.g. U.S. Pat. No. 5,304,121describes a hydrogel which releases the drug only after exposure to atriggering agent; U.S. Pat. No. 5,199,951 relies on thermal activation;according to U.S. Pat. No. 7,445,792 a lipophilic ̂hydration inhibitor'protects water-soluble drugs from premature release; and according toU.S. Pat. No. 5,370,614 a viscous matrix protects the drug frompremature release, however, the viscous matrix must be protected by asheath during the passage to the stenotic vessel segment. None of themethods has been tested in practice and proven to fulfill therequirements for fast, reliable and complete drug transfer to the targettissue. None of the methods has been designed to be used with scoring orcutting balloons.

Numerous methods of sustained drug release are known and successfullyused in practice but are not applicable to medical devices which are incontact with the target tissue for only a few seconds or minutes.Sustained drug release is usually achieved by embedding the drug in apolymer which restricts the diffusion rate to the surface and in thisway controls the transfer into the adjacent tissue.

Therefore, a need remains for a method or formulation which protects thecoating from premature losses during production, handling, and on theway to the lesion and still allows the immediate and complete release ofthe active ingredient at a location and point in time determined by theuser. During the production process this problem is even more severe forscoring and cutting balloons because of the more complex structure ofthe product. Scoring and cutting balloons have merits in the treatmentof certain lesions, e.g. if the conventional smooth balloons tend todislocate during inflation or if a controlled and predetermined injuryof the vessel wall is preferred to an uncontrolled dissection duringballoon inflation. Nevertheless, the problem of renarrowing of thevessel lumen due to excessive neointimal proliferation as a reaction tothe unavoidable injury during dilatation is the same as withconventional balloon catheters.

An advantageous way to control adherence and release of a drug from amedical device, e.g., an angioplasty balloon, is the selection of asuitable formulation and coating which do not require mechanicalprotection, or additional physical or chemical interaction with thecoating except the usual operation of the device e.g. inflation of afolded balloon to induce the release of the drug. Although desirable andfrequently tried, the conflicting objectives of perfect adherence duringproduction and before use and immediate release at the site of actionmake it a difficult task. A large variety of patent applications vaguelydisclose measures, compositions and devices to solve this problem forconventional balloon catheters either by the selection of drugs, thechoice of specific coating processes or formulations containing variousadditives. Long lists of compounds have been copied from textbooks ofchemistry, pharmacology, or pharmacy but even with extensiveexperimentation disclosures are not sufficiently clear to allow a personfamiliar with the subject and skilled in the art to come to asatisfactory solution without an inventive step. Examples of prior artare US 2008/0118544 reciting an excessive number of substances andsubstance classes or U.S. Pat. No. 7,445,795 which discloses the use ofhydration inhibitors' not applicable to the preferred class of verylipophilic drugs which require hydration enhancers' or ‘dispersion anddissolution enhancers’ as e.g. disclosed in WO 2004/028582. Although thehydrophilic additives (which may be regarded as ‘hydration enhancer’)work quite well on certain conventional balloon membranes (Scheller B,Speck U, Abramjuk C, Bernhardt U, Bohm M, Nickenig G. Paclitaxel ballooncoating—a novel method for prevention and therapy of restenosis.Circulation 2004; 110: 810-814) the adherence to various modernconventional or scoring PTA or PTCA balloons is either too weak or tootight resulting in premature loss of a major proportion of the drug orincomplete release at the target site. None of the known compositionshas been tried on scoring or cutting balloon catheters.

Antioxidants. In theory, antioxidants address an almost universalfeature of diseased tissue, namely the ‘reactive oxygen species’, andshould have widespread medical applications. In practice, only very fewcontrolled clinical trials have shown beneficial effects of antioxidants(Suzuki K. Antioxidants for therapeutic use: Why are only a few drugs inclinical use? Advanced Drug Delivery Reviews 2009;61:287-289).Antioxidants are mentioned as potentially useful drugs for the treatmentof focal vascular disease such as stenosis, restenosis, atheroscleroticplaques, and vulnerable plaques in US 2009/0136560 with no additive, inU.S. Pat. No. 5,571,523 as agents inducing apoptosis in vascular smoothmuscle cells, in WO 2004/022124 either as active drugs or as ̂hydrationinhibitors'. In US 2008/0241215 probucol, a drug approved for thetreatment of hyperlipidemia, a known risk factor for atheriosclerosis,is proposed as the active ingredient in stent coating, either alone orcombined with rapamycin or another anti-restenotic agent in aslow-release formulation. U.S. Pat. No. 6,211,247 claims pharmaceuticalcompositions containing an effective dose of resveratrol for preventingor treating various vascular pathologies following coronaryinterventions. Similarly, US 2007/0037739 discloses local deliverysystems comprising various bioactive agents including resveratrol whicheither alone or in the specified combinations are suitable for treatingor preventing abnormal luminal cell proliferation. None of theabove-mentioned documents contains data encouraging the use as additivesto a lipophilic drug to delay the release rate of the drug and nospecific compositions are disclosed which address the above-mentionedproblems of adhesion of a drug before the target lesion is reached andimmediate release when required.

Small proportions of antioxidants are commonly used to protect drugs ornutrients from decomposition by oxygen or oxidation, an applicationwhich has also been proposed for drugs coated on implantable medicaldevices such as stents (US 2007/0020380, US 2009/0246253) or ballooncatheters (US 2005/0037048, US 2009/0246252, especially paragraph [105]). However, antioxidants are commonly used in proportions of less than 1%by weight in relation to 100% by weight of the drug. Normally it isintended to use as less antioxidant as possible, i.e., less than 0.1% byweight in relation to 100% by weight of the drug (Voigt R. Lehrbuch derphar-mazeutischen Technologie. 5. Edition, Verlag Chemie,Wein-heim—Deerfield Beach, Fla.—Basel, 1984) . US 2005/0037048 disclosesa specific example which refers to a selected drug in a polymeric matrixrequiring an unusually high proportion of antioxidant.

Again, none of the above mentioned documents provides any hint to anadvantage in using antioxidants in combination with stable (i.e.oxidation-resistant drugs) and/or at dose levels which provide notherapeutic or prophylactic action.

Present invention. The problem underlying the present invention was theprovision of a scoring or cutting balloon catheter with an improvedadherence of the drug without negative effect on the release of the drugat the target site.

The problem was solved by a scoring or cutting balloon catheteraccording to claim 1. In other words, the problem was solved by ascoring or cutting balloon catheter carrying at least on a portion ofits surface at least one oxidation-insensitive drug oroxidation-insensitive polymer-free drug preparation and at least onelipophilic antioxidant at a ratio of 3-100% by weight of the at leastone lipophilic antioxidant in relation to 100% by weight of the drug,wherein the at least one oxidation-insensitive drug is selected oftaxanes, thalidomide, statins, corticoids and lipophilic derivatives ofcorticoids, and the at least one lipophilic antioxidant is selected ofnordihy-droguaiaretic acid, resveratrol and propyl gallate.“Polymer-free” means that no additional polymer is part of the coating.Preferred embodiments are disclosed in the dependant claims. Usually,antioxidants are used to stabilize oxidation-sensitive drugs againstdegradation by oxygen. They are considered useless in this regard if thedrug is stable against oxidative degradation, i.e. if the drug isoxidation-insensitive. Below, the terms “oxidation-insensitive drug”,“active drug” and “drug” are used interchangeable all meaning anoxidation-insensitive drug if the invention is concerned.

During testing of a large variety of coating methods, additives and drugcombinations the surprising discovery was made that certain lipophilicantioxidants added to less or even more lipophilic and more or lesswater soluble drugs, which are oxidation-insensitive, in a defined massratio significantly increase the adherence of the drug to scoring andcutting balloons during handling and on the way to the target lesioneven if the target lesion is located far away from the site where thedevice first enters a blood-filled introductory sheath, guiding catheteror vessel containing rapidly flowing blood. This was also tested withscoring balloons. In spite of the additional mechanical stress (ascompared to conventional balloons) imposed on the coating due themovement of the scoring wires surrounding the folded balloons the lossof the drug during the passage through a narrow hemostatic valve and acurved guiding catheter was very low. Thus, at least one lipophilicantioxidant in an amount of 3-100% by weight is used as an adherenceimprover for drugs coated on a scoring or cutting balloon catheterduring this initial step of introducing the medical device into thevasculature. The wording “at least one lipophilic antioxidant” meansthat single antioxidants but also mixtures of different antioxidants areincluded. Other substances or pharmaceutical compounds may be added tofurther adjust the properties of the product to the demand in respect ofstability or other pharmaceutical requirements and tolerance etc.

Examples of active drugs are inhibitors of cell proliferation,preferably taxanes such as paclitaxel, docetaxel and protaxel.Alternatively, specific inhibitors of neovascularization such asthalidomide, statins like atorvastatin, cerivastatin, fluvastatin oranti-inflammatory drugs like corticoids or even more preferredlipophilic derivatives of corticoids such as betamethasone diproprionateor dexa-methasone-21-palmitate are examples of oxidation-insensitivedrugs. Various drugs may be applied or combined if differentpharmacological actions are required or efficacy or tolerance is to beimproved. Thus, the wording “at least one drug or drug preparation”means that single drugs but also mixtures of different drugs areincluded. Preferred drugs are either lipophilic (partition coefficientbetween n-butanol and water >10, or display very poor water solubility(<1 mg/ml, 20° C.). Preferred are those drugs which in dry state arechemically stable during long-term storage without the addition of anantioxidant, e.g., paclitaxel and other taxanes, statins, thalidomide,corticosteroids and lipophilic derivatives of corticoids. Thereof, thepreferred ones are paclitaxel, protaxel and docetaxel with paclitaxelbeing the most preferred drug. Drugs must be used in a dose rangeproviding the desired effect without compromising the technical featuresof the coated balloon (balloon catheter) such as flexibility. Apreferred dose range is between 1 and 10 pg/mm² balloon surface, mostpreferred up to 6 g/mm².

The lipophilic antioxidants are antioxidants which are solid attemperatures up to 40° C. Preferred are nordihydroguaiaretic acid,propyl gallate and resveratrol, more preferred nordihydroguaiaretic acidand resveratrol, most preferred only resveratrol. Probucol is not apreferred additive.

Combinations of these antioxidants with the above-mentioned drugs showedan improved adherence. Different combinations, especially with otheroxidation-insensitive drugs, did not show a significantly improvedadherence or required very high amounts of the antioxidant which impairsthe mechanical features of the balloons (much more than 100% by weightin relation to 100% by weight of the drug).

Lipophilic antioxidant means that the partition coefficient of theantioxidant between n-butanol and water is >1, more preferred >10 andeven more preferred >100.

Preferably, the drug is more lipophilic than the antioxidant, i.e., thepartition coefficient between n-butanol and water of the drug is higherthan the partition coefficient between n-butanol and water of theantioxidant. If, however, an excipient prevents premature loss of thedrug from the medical device and/or enhances the fast and completetransfer to the tissue it shall not be excluded because of itsphysicochemical properties.

At the dose density used the chosen antioxidants do not display relevanttherapeutic or prophylactic effects in respect of the disease which istreated by the coated medical device nor is the relative amount of theantioxidant chosen to protect the drug from oxidative decomposition.This means that a non-bioactive dose of the antioxidant is pre-ferred.The dose density and the mass relation of the antioxidant to the drugare solely optimized in respect of adherence of the drug to and releasefrom the medical device surface. The antioxidant dose on the medicaldevice is too low to provide the desired pharmacological effect, i.e.,it is ineffective on its own. The antioxidant on the medical device isnot required to protect the active drug (e.g., the antiproliferativedrug) from oxidative decomposition during production, sterilization andstorage; at least it is not required at the dose or concentrationapplied according to this invention. ^(3/4)Not required' means that theactive drug is stable enough without the antioxidant or at anantioxidant dose or dose density or ratio to the active drug below thedose according to the present invention. Sufficient stability' meansthat less than 5% of the active drug is lost due to oxidativedecomposition between the coating of the device and the use in patientsone year after production if stored at ambient temperature (=drug ordrug preparation stable against oxidative decomposition, air-oxygenexposure not excluded). In conclusion the invention relates to acombination of an antioxidant with a drug which needs no protection fromoxidative decomposition or at least a dose of the antioxidant whichsurpasses the amount of antioxidant required protecting the drug fromoxidation by its antioxidant action. The antioxidant serves as additiveor excipient not functioning as a stabilizer for an oxidation-sensitivebiologically active ingredient (drug) nor displaying a therapeutic orprophylactic effect on its own at the selected dose.

The dose of the antioxidant on the surface of a medical device may bedefined in respect of the therapeutic drug. Preferred relationships(weight/weight) are 3-100% antioxi-dant of the weight of the drug. Forexample, if the dose density of the drug is 5 g/mm² device surface, theamount of antioxidant is 0.15-5.0 g/mm². Higher proportions of theantioxidant may be selected if either the drug is applied at a dosebelow 3 pg/mm² device surface or the adherence of the drug to the devicesurface is further improved. The antioxidant load of the device mayreach 10 g/mm². A higher load is possible. Other preferred ranges forthe relationship of antioxidant to drug on a weight/weight basis are5-100%, more preferred 10-100%, and even more preferred 20-100% and mostpreferred 50-100% in relation to 100% of the drug. Especially the rangeof 50-100% on a weight/weight basis enhances the adherence significantly(see Example 3). The relationship may also be defined in respect ofmoles: in a preferred embodiment the antioxidant is present from 10 mole% relative to the drug to 200 mole %.

Higher amounts of the antioxidant may be useful; they may be onlyexcluded if they display on their own significant pharmacologicalprophylactic or therapeutic effects in respect of the disease to betreated.

If more than one drug is used the total weight of the drugs or the totalmoles of the drugs serve as basis for the calculation of the amount ofthe antioxidant. If more than one antioxidant is used the total weightof the antioxidants or the total moles of the antioxidants serve asbasis for the calculation of the amount of the antioxidants.

Other well tolerated and approved additives and/or excipi-ents may beapplied to further improve the mechanical or pharmaceutical propertiesof the coating. Polymer-free coating compositions are preferred. It is aspecial advantage of the present compositions that they do not requirethe use of polymers to prevent premature release of the drug.Nevertheless, small amounts of pharmaceutically acceptable polymers suchas polyacrylic acids may be added, e.g., to improve the distribution ofthe drug on the balloon or adherence of the dry coating during handling.Small amounts mean about 1-20% by weight in relation to 100% by weightof the drug(s). If polymers are used substances with low to moderatemolecular weight, i.e., 2000 to 50 000 D are preferred.

Usually, drugs and mixtures of drugs with additives are coated onmedical devices as liguid formulations in volatile solvents, accordingto the current invention preferably without addition of a polymer, i.e.polymer-free. The choice of solvent is important for the distribution ofthe drug on the device, especially if the device is coated at anadvanced stage of production. An advanced stage of production of ascoring or cutting balloon may include the scoring or cutting elementsof the device, the structures required to fix these elements and analready folded balloon. The solvents further determine the structure ofthe coating in dry state and the adherence and release of the drug fromthe surface. Preferred organic solvents are acetone, tetrahydrofuran,and various alcohols such as methanol and ethanol. Usually, 1 to 30%(volume/volume) water is added. The drug or drugs and the antioxidantmay be applied at the same time dissolved in the same solvent or mixtureof solvents. Alternatively, they may be separately dissolved in the sameor different solvents and sequentially applied. The solution (s) is/arepolymer-free in either case. In a preferred embodiment, the scoring orcutting balloon catheter has been polymer-free coated with at least oneoxidation-insensitive drug and at least one antioxidant both togetherdissolved in tetrahydrofuran or a mixture of solvents containing morethan 25% (v/v) tetrahy-drofuran or each separately dissolved optionallyselecting a different solvent for the at least one lipophilicantioxidant. Another preferred embodiment is based on a scoring orcutting balloon catheter, which has been polymer-free coated with atleast one oxidation-insensitive drug and at least one antioxidant bothtogether dissolved in acetone or a mixture of solvents containing morethan 25% (v/v) acetone or each separately dissolved optionally selectinga different solvent for the at least one lipophilic antioxidant. Coatingwith dry particles such as micro- or nano-particles, crystals, capsulesetc. or particles suspended in a liquid preparation is possible. Coatingwith particles may be facilitated by a roughened or sticky surface ofthe medical device.

A variety of coating procedures providing more or less uniform layers onmedical devices are known from the literature and are disclosed inpatent applications. These include simple dipping, spraying, and methodsproviding precise doses and homogeneous distributions (e.g., WO2009/018816). Coating may be applied stepwise, either as multiple layersof the same composition or as layers with different compositions e.g.the drug first and the antioxidant second or in the opposite order. Allthese methods may be applied to the formulations of the currentinvention. The sequential coating with, e.g., (a) the drug first and (b)second the antioxidant dissolved in a solvent in which the drug ispoorly soluble by, e.g., spraying results in substantially separatelayers. This is completely different from the application ofantioxidants for chemical protection of oxidation sensitive drugs whichrequires a homogeneous mixing of the antioxidant with the drug.

Thus, a preferred embodiment of the present invention is a scoring orcutting balloon catheter, which has been polymer-free sequentiallycoated with at least one oxidation-insensitive drug and at least onelipophilic antioxidant in a way that the oxidation-insensitive drug andthe antioxidant are not homogeneously mixed.

Furthermore, coated scoring or cutting balloon catheter may be driedunder different conditions such as temperature, air flow, gascomposition, and pressure at different stages of the production process.They may be stored in water-vapor-tight seals with a separately packedwater absorbing-agent within the seal.

Subject of the current invention are scoring or cutting ballooncatheters, e.g., catheters for angioplasty or coronary angioplasty.Preferred are scoring or cutting balloon catheters for short-lasting useduring an interventional image guided therapy. Short lasting use meansthat the device is not implanted but eliminated from the body when theprocedure is finished, usually within less than 10 minutes, but neverlater than a few, preferably 5, hours after the end of the procedure.Catheters may contain balloon membranes made from various polymers andcopolymers , polyam-ides (nylon 12, pebax), polyethylenes,polyurethanes, various polyvinyls and the like. Independently of thetype of material, the adherence and release properties of drugs areimproved by the addition of lipophilic antioxidants. Furthermore,catheters comprise elements which are aimed at scoring or cutting thesurfaces in direct contact with the inflated balloons, e.g. wires withvarious profiles, or protrusions of the balloon surface.

The scoring or cutting balloon catheter carries the at least one drug ordrug preparation and the at least one lipophilic antioxidant at least ona portion of its surface which is aimed at coming into close contactwith the tissue to be treated, e.g., the balloon at the distal portionof a catheter shaft. This means that at least 5%, preferably more than50%, most preferably more than 90% of the surface is coated. The balloonof a scoring or cutting balloon catheter has a central cylindrical partand two opposite conical ends. If less than 100% of the ballooncatheter's surface is coated, it is preferred that the cylindrical partis coated and that at least parts of or the complete conical ends remainuncoated.

Another embodiment is a scoring or cutting balloon catheter carrying atleast on a portion of its surface polymer-free at least one Limus drugor Limus drug preparation and at least one lipophilic antioxidant, whichis nordihydroguaia-retic acid or resveratrol, preferably resveratrol, ata ratio of 3-100% by weight of the at least one lipophilic antioxidantin relation to 100% by weight of the drug.

Preferably, the Limus drug is an mTOR inhibitor, more preferablyselected from sirolimus, everolimus, zotarolimus, biolimus andtemsirolimus, most preferred sirolimus. Concerning preferred ways ofcarrying out this embodiment, the same applies as described above withrespect to the combination of oxidation-insensitive drugs/drugpreparations and lipophilic antioxidants.

Below, the invention is described by means of Examples.

EXAMPLE 1

Balloons for percutaneous transluminal coronary angioplasty type A(AngioSculpt 3.5-20 mm, AngioScore, Inc., Fremont Calif., USA) werecoated either with paclitaxel alone or combined with iopromide(iodinated contrast agent according to WO 02/076509) or differentamounts of butylated hydroxy-toluene (BHT); solvent: acetone/ethanol/H2O. Coated balloons were tested in respect of paclitaxel loss duringthe passage through a hemostatic valve, Medtronic Launcher JL 3.5 6Fguiding catheter and one minute in stirred blood (37° C.). When admixedat sufficient concentration to the coating solution, BHT improved theadhesion of paclitaxel.

Loss on the way to the Catheter lesion Coating solution labeling % ofdose No additive 1 24 2 40 Iopromide as an addi- 3 49 tive; ca. 0.5mg/mg 4 34 paclitaxel BHT 5% = 0.05 mg 5 15 BHT/mg paclitaxel 6 26 BHT24% = 0.24 mg 7 10 BHT/mg paclitaxel 8  6

EXAMPLE 2

Balloons for percutaneous transluminal coronary angioplasty type A werecoated either with paclitaxel alone or combined with iopromide(iodinated contrast agent according to WO 02/076509), see example 2, orbutylated hydroxytoluene (BHT) or nordihydroguaiaretic acid. Coatedballoons were tested in respect of paclitaxel loss during the passagethrough a hemostatic valve, a Medtronic Launcher JL 3.5 6F guidingcatheter and in stirred blood (37° C.) for one minute. When admixed atsufficient concentration to the coating solution, lipophilicantioxidants improve the adhesion of paclitaxel whereas the releaseduring balloon inflation in a coronary artery (determined in separateexperiments) was not impaired.

Loss on Residual the way to paclitaxel Label- the lesion on balloonsCoating solution ing % of dose % of dose No additive Control 32 no dataacetone/ethanol/H₂O 1, 2 Iopromide as an addi- tive; ca. 0.5 mg/mgpaclitaxel; Control 42 ~10 acetone/ethanol/H₂O 3, 4 BHT 24% = 0.24 mgBHT/ A 15.3 ± 9.5    11 mg paclitaxel; acetone/ ethanol/H₂O BHT 24% =0.24 mg BHT/ B 3.4 ± 4.8   13 mg paclitaxel; tetrahydrofuran/ethanol/H₂O Nordihydroguaiatetic acid C 4.2 ± 7.2 no data 35% = 0.35mg/mg paclitaxel; acetone/ethanol/ H₂O

EXAMPLE 3

Balloons for percutaneous transluminal coronary angioplasty type A werecoated either with paclitaxel without resveratrol or combined withresveratrol. Coated balloons were tested in respect of paclitaxel lossas described in example 1. When admixed at sufficient concentration tothe coating solution, resveratrol improved the adhesion of paclitaxel.

Loss on the way to the lesion Coating solution Labeling % of doseResveratrol 0% acetone/ Control 25 ± 8  tetrahydrofuran/H₂O Resveratrol20% = 0.2 mg/ N 21 ± 6  mg paclitaxel; acetone/ tetrahydrofuran/H₂OResveratrol 50% = 0.5 mg/ O  7 ± 11 mg paclitaxel; acetone/tetrahydrofuran/H₂O

EXAMPLE 4

Balloons for percutaneous transluminal coronary angioplasty type A werecoated in already folded condition either with paclitaxel without orwith polyacrylic acid. Polyacrylic acid (molecular weight about 6000 D(Polysciences Inc., USA) and glycerol improved the homogeneity of thecoating on the balloon.

Distribution on Coating solution Labeling balloons Paclitaxel withoutpoly- N Spreading limited acrylic acid acetone/ to directlytetrahydrofuran/H₂O accessible surface 0.08 mg polyacrylic D Irregulardistri- acid + 0.06 mg glycerol/ bution, partly mg paclitaxel acetone/below the folds tetrahydrofuran/H₂O 0.15 mg polyacrylic acid + E Almost0.06 mg glycerol/mg homogeneous paclitaxel in acetone/ distributiontetrahydrofuran/H₂O including areas below the folds

1. Scoring or cutting balloon catheter carrying at least on a portion ofits surface at least one oxidation-insensitive drug oroxidation-insensitive polymer-free drug preparation and at least onelipophilic antioxidant at a ratio of 3-100% by weight of the at leastone lipophilic antioxidant in relation to 100% by weight of the drug,wherein the at least one oxidation-insensitive drug is selected oftaxanes, thalidomide, statins, cor-ticoids and lipophilic derivatives ofcorticoids, and the at least one lipophilic antioxidant is selected ofnordihydroguaiaretic acid, resveratrol and propyl gallate.
 2. Scoring orcutting balloon catheter according to claim 1, wherein the at least onelipophilic antioxidant is contained at a ratio of 5-100% by weight,preferably at a ratio of 10-100% by weight, more preferred at a ratio of20-100% by weight, and even more preferred at a ratio of 50-100% byweight in relation to 100% by weight of the at least one drug. 3.Scoring or cutting balloon catheter according to claim 1, wherein the atleast one oxidation-insensitive drug is more lipophilic than theantioxidant.
 4. Scoring or cutting balloon catheter according to any oneof claim 1, wherein the taxane is selected of paclitaxel, protaxel ordocetaxel and is preferably paclitaxel.
 5. Scoring or cutting ballooncatheter according to any one of claim 1, wherein the statin is selectedof atorvastatin, cerivastatin or fluvastatin ; the corticoid or thelipophilic derivative of the corticoid is selected of betamethasonedipropionat or dexamethasone-21-palmitate .
 6. Scoring or cuttingballoon catheter according to any one of claim 1, wherein the at leastone antioxidant load is up to 10 g/mm² of coated catheter surface. 7.Scoring or cutting balloon catheter according to any one of claim 1,wherein the at least one antioxidant is nordihydroguaiaretic acid orresveratrol, preferably resveratrol.
 8. Scoring or cutting ballooncatheter according to any one of claim 1, which has been polymer-freecoated with at least one oxidation-insensitive drug and at least oneantioxidant both together dissolved in tetrahydrofuran or a mixture ofsolvents containing more than 25% (v/v) tetrahydrofuran or eachseparately dissolved optionally selecting a different solvent for the atleast one lipophilic antioxidant.
 9. Scoring or cutting balloon catheteraccording to any one of claim 1, which has been polymer-free coated withat least one oxidation-insensitive drug and at least one antioxidantboth together dissolved in acetone or a mixture of solvents containingmore than 25% (v/v) acetone or each separately dissolved optionallyselecting a different solvent for the at least one lipophilicantioxidant.
 10. Scoring or cutting balloon catheter according to anyone of claims 1, which has been polymer-free sequentially coated with atleast one oxidation-insensitive drug and at least one lipophilicantioxidant in a way that the oxidation-insensitive drug and theantioxidant are not homogeneously mixed.
 11. Scoring or cutting ballooncatheter carrying at least on a portion of its surface polymer-free atleast one Limus drug or Limus drug preparation and at least onelipophilic antioxidant, which is nordihydroguaiaretic acid orresveratrol, preferably resveratrol, at a ratio of 3-100% by weight ofthe at least one lipophilic antioxidant in relation to 100% by weight ofthe drug.
 12. Scoring or cutting balloon catheter according to claim 11,wherein the at least one Limus drug is an mTOR inhibitor, preferablyselected from sirolimus, everolimus, zotarolimus, biolimus andtemsirolimus , more preferably sirolimus.